N<Subscript>2</Subscript>O emission from conventional and minimum-tilled soils

In this study, we investigated N₂O emissions from two fields under minimum tillage, cropped with maize (MT maize) and summer oats (MT oats), and a conventionally tilled field cropped with maize (CT maize). Nitrous oxide losses from the MT maize and MT oats fields (5.27 and 3.64 kg N₂O-N ha⁻¹, respectively) were significantly higher than those from the CT maize field (0.27 kg N₂O-N ha⁻¹) over a period of 1 year. The lower moisture content in CT maize (43% water-filled pore space [WFPS] compared to 60–65%) probably caused the difference in total N₂O emissions. Denitrification was found to be the major source of N₂O loss. Emission factors calculated from the MT field data were high (0.04) compared to the CT field (0.001). All data were simulated with the denitrification decomposition model (DNDC). For the CT field, N₂O and N₂O + N₂ emissions were largely overestimated. For the MT fields, there was a better agreement with the total N₂O and N₂O + N₂ emissions, although the N₂O emissions from the MT maize field were underestimated. The simulated N₂O emissions were particularly influenced by fertilization, but several other measured N₂O emission peaks associated with other management practices at higher WFPS were not captured by the model. Several mismatches between simulated and measured \textNH₄⁺ {\text{NH}}_4^ + , \textNO₃^- {\text{NO}}_3^ - and WFPS for all fields were observed. These mismatches together with the insensitivity of the DNDC model for increased N₂O emissions at the management practices different from fertilizer application explain the limited similarity between the simulated and measured N₂O emissions pattern from the MT fields.     

Methane fluxes and nitrogen dynamics from a drained fenland peat

 Rates of methane uptake were measured in incubation studies with intact cores from adjacent fenland peats that have been under arable management and woodland management for at least the past 30 years. On two separate occasions the woodland peat showed greater rates of uptake than the arable peat. These rates ranged from 23.1 to 223.3 μg CH₄ m^–2 day^–1 for the woodland peat and from 29.6 to 157.6 μg CH₄ m^–2 day^–1 for the arable peat. When the peats were artificially flooded there was a decrease in the rate of methane oxidation, but neither site showed any net efflux of methane. ¹⁵N isotopic dilution was used to characterise nitrogen cycling within the two peats. Both showed similar rates of gross nitrogen mineralisation (3.58 mg N kg^–1 day^–1, arable peat; 3.54 N kg^–1 day^–1, woodland peat) and ammonium consumption (4.19 arable peat and 4.70 mg N kg^–1 day^–1 woodland peat). There were significant differences in their inorganic ammonium and nitrate pool sizes, and the rate of gross nitrification was significantly higher in the woodland peat (4.90 mg N kg^–1 day^–1) compared to the arable peat (1.90 mg N kg^–1 day^–1). These results are discussed in the light of high atmospheric nitrogen deposition. Received: 1 December 1997     

Comparison of two versions of the acetylene inhibition/soil core method for measuring denitrification loss from an irrigated wheat field

 Two versions of the acetylene inhibition (AI)/soil core method were compared for the measurement of denitrification loss from an irrigated wheat field receiving urea-N at a rate of 100 kg ha^–1. With AI/soil core method A, the denitrification rate was measured by analysing the headspace N₂O, followed by estimation of N₂O dissolved in the solution phase using Bunsen absorption coefficients. With AI/soil core method B, N₂O entrapped in the soil was measured in addition to that released from soil cores into the headspace of incubation vessels. In addition, the two methods were also compared for measurement of the soil respiration rate. Of the total N₂O produced, 6–77% (average 40%) remained entrapped in the soil, whereas for CO₂, the corresponding figures ranged from 12–65% (average 44%). The amount of the entrapped N₂O was significantly correlated with the water-filled pore space (WFPS) and with the N₂O concentration in the headspace, whereas CO₂ entrapment was dependent on the headspace CO₂ concentration but not on the WFPS. Due to the entrapment of N₂O and CO₂ in soil, the denitrification rate on several (18 of the 41) sampling dates, and soil respiration rate on almost all (27 of the 30) sampling dates were significantly higher with method B compared to method A. Averaged across sampling dates, the denitrification rate measured with method B (0.30 kg N ha^–1 day^–1) was twice the rate measured with method A, whereas the soil respiration rate measured with method B (34.9 kg C ha^–1 day^–1) was 1.6 times the rate measured with method A. Results of this study suggest that the N₂O and CO₂ entrapped in soil should also be measured to ensure the recovery of the gaseous products of denitrification by the soil core method. Received: 12 May 1998     

Mineralization and denitrification in upland, nearly saturated and flooded subtropical soil I. Effect of nitrate and ammoniacal nitrogen

 The influence of fertilizer N applied through nitrate and ammoniacal sources on the availability of nitrate, supply of C, and gaseous N losses via denitrification (using acetylene inhibition technique) in a semiarid subtropical soil (Typic Ustochrepts) was investigated in a growth chamber simulating upland [60% water-filled pore space (WFPS)], nearly saturated (90% WFPS), and flooded (120% WFPS) conditions. The rate of denitrification was very low in the upland soil conditions, irrespective of fertilizer N treatments. Increasing water content to nearly saturated and flooded conditions resulted in four- to sixfold higher rates of denitrification within 2 days, suggesting that the denitrifying activity commences quickly. Results of this study reveal that (1) under restricted aeration, these soils could support high rates of denitrification (∼6 mg N kg^–1 day^–1) for short periods when nitrate is present; (2) application of fertilizer N as nitrate enhances N losses via denitrification (∼10 mg N kg^–1 day^–1) – however, the supply of available C determines the intensity and duration of denitrification; (3) when fertilizer N is applied as an ammoniacal form, nitrification proceeds slowly and nitrate availability limits denitrification in flooded soil; (4) the nearly saturated soil, being partially aerobic, supported greater nitrification of applied ammoniacal fertilizer N than flooded soil resulting in higher relative rates of denitrification; and (5) under aerobic soil conditions, 26 mg mineral N kg^–1 accumulated in control soil over a 16-day period, demonstrating a modest capacity of such semiarid subtropical soils, low in organic matter, to supply N to growing plants. Received: 7 June 1999     

Soil N<Subscript>2</Subscript>O emissions and N<Subscript>2</Subscript>O/(N<Subscript>2</Subscript>O+N<Subscript>2</Subscript>) ratio as affected by different fertilization practices and soil moisture

The objective of this work was to evaluate the effect of the chemical nature and application frequency of N fertilizers at different moisture contents on soil N₂O emissions and N₂O/(N₂O+N₂) ratio. The research was based on five fertilization treatments: unfertilized control, a single application of 80 kg ha⁻¹ N-urea, five split applications of 16 kg ha⁻¹ N-urea, a single application of 80 kg ha⁻¹ N–KNO₃, five split applications of 16 kg ha⁻¹ N–KNO₃. Cumulative N₂O emissions for 22 days were unaffected by fertilization treatments at 32% water-filled pore space (WFPS). At 100% and 120% WFPS, cumulative N₂O emissions were highest from soil fertilized with KNO₃. The split application of N fertilizers decreased N₂O emissions compared to a single initial application only when KNO₃ was applied to a saturated soil, at 100% WFPS. Emissions of N₂O were very low after the application of urea, similar to those found at unfertilized soil. Average N₂O/(N₂O+N₂) ratio values were significantly affected by moisture levels (p = 0.015), being the lowest at 120% WFPS. The N₂O/(N₂O+N₂) ratio averaged 0.2 in unfertilized soil and 0.5 in fertilized soil, although these differences were not statistically significant.     

Processes responsible for the nitrous oxide emission from a Costa Rican Andosol under a coffee agroforestry plantation

We used the inhibitor acetylene (C₂H₂) at partial pressures of 10 Pa and 10 kPa to inhibit autotrophic nitrification and the reduction of nitrous oxide (N₂O) to N₂, respectively. Soils (Andosol) from a Coffea arabica plantation shaded by Inga densiflora in Costa Rica were adjusted to 39, 58, 76 and 87% water-filled pore space (WFPS) and incubated for 6 days in the absence or presence of C₂H₂. Soil respiration, nitrification rates and N₂O emissions by both processes were measured in relation to soil moisture conditions. At all WFPS studied, rates of N₂O and N₂ productions were small (4.8; 14.7; 23 and 239.6 ng N–N₂O g⁻¹ d.w. d⁻¹ at 39, 58, 76 and 87% WFPS, respectively), and despite a low soil pH (4.7), N₂O was mainly produced by nitrification, which was responsible for 85, 91, 84 and 87% of the total N₂O emissions at 39, 58, 76 and 87% WFPS, respectively. At the three smaller values of WFPS, a linear relationship was established between WFPS, soil respiration, nitrification and N₂O released by nitrification; no N₂ was produced by denitrification. At more anaerobic conditions achieved by a WFPS of 87%, a large rate of N₂O production was measured during nitrification, and N₂ production accounted for 84% of the gaseous N fluxes caused by denitrification.     

Denitrification and total fertilizer-N losses from an irrigated cotton field

 In a 2-year field study, denitrification loss was measured from an irrigated sandy-clay loam under cotton receiving urea-N at 158–173 kg ha^–1. An acetylene inhibition-soil core method was employed for the direct measurement of denitrification, considering also the N₂O entrapped in the soil. Taking into account the N₂O evolved from soil cores and that entrapped in the soil, a total of 65.7 kg N ha^–1 and 64.4 kg N ha^–1 was lost due to denitrification during the 1995 and 1996 cotton-growing seasons, respectively. Most (>70%) of the denitrification loss occurred during June–August, a period characterized by high soil temperatures and heavy monsoon rains. On average, 35% of the denitrification-N₂O was found entrapped in the soil and the amount of entrapped N₂O was significantly correlated with head space N₂O concentration and with water-filled pore space. ¹⁵N-balance during the 1996 growing season revealed a loss of 71.8 kg N ha^–1. It was concluded that a substantial proportion of the fertilizer-N applied to irrigated cotton is lost under the semiarid subtropical climatic conditions prevailing in the Central Punjab region of Pakistan and that denitrification is the major N loss process under irrigated cotton in this region. Received: 8 March 1999     

Nitrous oxide emissions from a fallow and wheat field as affected by increased soil temperatures

 In order to determine the effects of increased soil temperature resulting from global warming on microbiological reactions, a 21-month field experiment was carried out in the Bavarian tertiary hills. The major objective was to focus on N₂O releases as either a positive or negative feedback in response to global warming. The soils of a fallow field and a wheat field were heated 3  °C above ambient temperature and N₂O fluxes were measured weekly from June 1994 to March 1996. During the experimental period, measured temperature differences between the control plots and the heated plots were 2.9±0.3  °C at a depth of 0.01 m and 1.0–1.8  °C at a depth of 1 m. Soil moisture decreased with the elevated soil temperatures of the heated plots. The mean differences in soil moisture between the treatments were 6.4% (fallow field) and 5.2%_DW (wheat field dry weight, DW), respectively. Overall N₂O releases during the experimental period from the fallow field were 4.8 kg N₂O–N ha^–1 in the control plot against 5.0 kg N₂O–N ha^–1 in the heated plot, and releases from the wheat field were 8.0 N₂O–N ha^–1 in the control plot and 7.6 N₂O–N kg ha^–1 in the heated plot. However, on a seasonal basis, cumulated N₂O emissions differed between the plots. During the summer months (May–October), releases from the heated fallow plot were 3 times the rates from the control plot. In the winter months, N₂O releases increased in both the fallow and wheat fields and were related to the number of freezing and thawing cycles. Received: 1 December 1997     

Emissions of nitrous oxide from a constructed wetland using a groundfilter and macrophytes in waste-water purification of a dairy farm

 In less populated rural areas constructed wetlands with a groundfilter made out of the local soil mixed with peat and planted with common reed (Phragmites australis) are increasingly used to purify waste water. Particularly in the rhizosphere of the reed, nitrification and denitrification processes take place varying locally and temporally, and the question arises to what extent this type of waste-water treatment plant may contribute to the release of N₂O. In situ N₂O measurements were carried out in the two reed beds of the Friedelhausen dairy farm, Hesse, Germany, irrigated with the waste water from a cheese dairy and 70 local inhabitants (12 m³ waste water or 6 kg BOD₅ or 11 kg chemical O₂ demand (COD_Mn) day^–1). During November 1995 to March 1996, the release of N₂O was measured weekly at 1 m distances using eight open chambers and molecular-sieve traps to collect and absorb the emitted N₂O. Simultanously, the N₂O trapped in the soil, the soil temperature, as well as the concentrations of NH₄ ⁺-N, NO₃ ^–-N, NO₂ ^–-N, water-soluble C and the pH were determined at depths of 0–20, 20–40 and 40–60 cm. In the waste water from the in- and outflow the concentrations of COD_Mn, BOD₅, NH₄ ⁺-N, NO₃ ^–-N, NO₂ ^–-N, as well as the pH, were determined weekly. Highly varying amounts of N₂O were emitted at all measuring dates during the winter. Even at soil temperatures of –1.5  °C in 10 cm depth of soil or 2  °C at a depth of 50 cm, N₂O was released. The highest organic matter and N transformation rates were recorded in the upper 20 cm of soil and in the region closest to the outflow of the constructed wetland. Not until a freezing period of several weeks did the N₂O emissions drop drastically. During the period of decreasing temperatures less NO₃ ^–-N was formed in the soil, but the NH₄ ⁺-N concentrations increased. On average the constructed wetlands of Friedelhausen emitted about 15 mg N₂O-N inhabitant equivalent^–1 day^–1 during the winter period. Nitrification-denitrification processes rather than heterotrophic denitrification are assumed to be responsible for the N₂O production. Received: 28 October 1998     

Crop residues and fertilizer nitrogen influence residue decomposition and nitrous oxide emission from a Vertisol

Crop residues with high C/N ratio immobilize N released during decomposition in soil, thus reducing N losses through leaching, denitrification, and nitrous oxide (N₂O) emission. A laboratory incubation experiment was conducted for 84 days under controlled conditions (24°C and moisture content 55% of water-holding capacity) to study the influence of sugarcane, maize, sorghum, cotton and lucerne residues, and mineral N addition, on N mineralization–immobilization and N₂O emission. Residues were added at the rate of 3 t C ha⁻¹ to soil with, and without, 150 kg urea N ha⁻¹. The addition of sugarcane, maize, and sorghum residues without N fertilizer resulted in a significant immobilization of soil N. Amended soil had significantly (P < 0.05) lower NO₃⁻–N, which reached minimum values of 2.8 mg N kg⁻¹ for sugarcane (at day 28), 10.3 mg N kg⁻¹ for maize (day 7), and 5.9 mg N kg⁻¹ for sorghum (day 7), compared to 22.7 mg N kg⁻¹ for the unamended soil (day 7). During 84 days of incubation, the total mineral N in the residues + N treatments were decreased by 45 mg N kg⁻¹ in sugarcane, 34 mg kg⁻¹ in maize, 29 mg kg⁻¹ in sorghum, and 16 mg kg⁻¹ in cotton amended soil compared to soil + N fertilizer, although soil NO₃⁻–N increased by 7 mg kg⁻¹ in lucerne amended soil. The addition of residues also significantly increased amended soil microbial biomass C and N. Maximum emissions of N₂O from crop residue amended soils occurred in the first 4–5 days of incubation. Overall, after 84 days of incubation, the cumulative N₂O emission was 25% lower with cotton + N fertilizer, compared to soil + N fertilizer. The cumulative N₂O emission was significantly and positively correlated with NO₃⁻–N (r = 0.92, P < 0.01) and total mineral N (r = 0.93, P < 0.01) after 84 days of incubation, and had a weak but significant positive correlation with cumulative CO₂ in the first 3 and 5 days of incubation (r = 0.59, P < 0.05).     

Relationship between nitrous oxide emission and winter wheat production

A 3-year field study in southeast China was performed to examine the relationship between N₂O emission and winter wheat production. Over the 2002–03, 2003–04 and 2004–05 wheat-cropping seasons, N₂O emissions depended on nitrogen addition, plowing practice, and preceding crop type treatments, and showed a pronounced inter-annual variation. N₂O–N emission factor, the proportion of fertilizer N released as N₂O–N from the wheat field, varied from 1.33% to 2.97%. The relationship between N₂O emission (y) and crop yield (x) was well explained by the function y = 3.773Ln(x) + 1.46. Similarly, the function y = 4.445Ln(x) − 3.52 can be employed to address the relationship between N₂O emission (y) and above ground biomass (x). About 84% and 87% of variation in seasonal N₂O emission were explained by the two functions, while only 66% of the variation was represented by the N input with a linear relationship. The results of this study suggest that seasonal N₂O emission of soil under winter wheat could be better predicted by crop yield and biomass than by N input. Submitted to Biology and Fertility of Soils.     

Mechanisms of N2O and NO production in the soil profile of a drained and forested peatland, as studied with acetylene, nitrapyrin and dimethyl ether

 Acetylene, dimethyl ether (DME) and 2-chloro-6-trichloromethyl pyridine (nitrapyrin) were used as inhibitors to study the contributions of nitrification and denitrification to the production of N₂O and nitric oxide (NO) in samples taken from the soil profile of a peatland drained for forestry. Acetylene and DME inhibited 60–100% of the nitrification activity in field-moist samples from the 0–5 cm and 5–10 cm peat layers, whereas nitrapyrin had no inhibitory effect. In the 0–5 cm peat layer the N₂O production could be reduced by up to 90% with inhibitors of nitrification, but in the 5–10 cm peat layer this proportion was 20–30%. All the inhibitors removed 96–100% of the nitrification potential in peat-water slurries from the 0–5 cm peat layer, but the 5–10 cm layer had a much lower nitrification activity, and here the efficiency of the inhibitors was more variable. Litter was the main net source of NO in the peat profile. NO₃ ^– production was lower in the litter layer than in the peat, whereas N₂O production was much higher in the litter than in the peat. Denitrification was the most probable source of N₂O and NO in the litter, which had a high availability of organic substrates. Received: 14 July 1997     

The effect of reduced tillage on nitrous oxide emissions of silt loam soils

The effect of reduced tillage (RT) on nitrous oxide (N₂O) emissions of soils from fields with root crops under a temperate climate was studied. Three silt loam fields under RT agriculture were compared with their respective conventional tillage (CT) field with comparable crop rotation and manure application. Undisturbed soil samples taken in September 2005 and February 2006 were incubated under laboratory conditions for 10 days. The N₂O emission of soils taken in September 2005 varied from 50 to 1,095 μg N kg⁻¹ dry soil. The N₂O emissions of soils from the RT fields taken in September 2005 were statistically (P < 0.05) higher or comparable than the N₂O emissions from their respective CT soil. The N₂O emission of soils taken in February 2006 varied from 0 to 233 μg N kg⁻¹ dry soil. The N₂O emissions of soils from the RT fields taken in February 2006 tended to be higher than the N₂O emissions from their respective CT soil. A positive and significant Pearson correlation of the N₂O–N emissions with nitrate nitrogen (NO₃ ⁻–N) content in the soil was found (P < 0.01). Leaving the straw on the field, a typical feature of RT, decreased NO₃ ⁻–N content of the soil and reduced N₂O emissions from RT soils.     

Attenuation of Nitrogen,Phosphorus and <Emphasis Type="Italic">E. coli</Emphasis> Inputs from Pasture Runoff to Surface Waters by a Farm Wetland: the Importance of Wetland Shape and Residence Time

Water quantity and quality were monitored for 3 years in a 360-m-long wetland with riparian fences and plants in a pastoral dairy farming catchment. Concentrations of total nitrogen (TN), total phosphorus (TP) and Escherichia coli were 210–75,200 g N m⁻³, 12–58,200 g P m⁻³ and 2–20,000 most probable number (MPN)/100 ml, respectively. Average retentions (±standard error) for the wetland over 3 years were 5 ± 1%, 93 ± 13% and 65 ± 9% for TN, TP and E. coli, respectively. Retentions for nitrate–N, ammonium–N, filterable reactive P and particulate C were respectively −29 ± 5%, 32 ± 10%, −53 ± 24% and 96 ± 19%. Aerobic conditions within the wetland supported nitrification but not denitrification and it is likely that there was a high conversion rate from dissolved inputs of N and P in groundwater, to particulate N and P and refractory dissolved forms in the wetland. The wetland was notable for its capacity to promote the formation of particulate forms and retain them or to provide conditions suitable for retention (e.g. binding of phosphate to cations). Nitrogen retention was generally low because about 60% was in dissolved forms (DON and NO_X–N) that were not readily trapped or removed. Specific yields for N, P and E. coli were c. 10–11 kg N ha⁻¹ year⁻¹, 0.2 kg P ha⁻¹ year⁻¹ and ≤10⁹ MPN ha⁻¹ year⁻¹, respectively, and generally much less than ranges for typical dairy pasture catchments in New Zealand. Further mitigation of catchment runoff losses might be achieved if the upland wetland was coupled with a downslope wetland in which anoxic conditions would promote denitrification.     

Influence of soil properties on the turnover of nitric oxide and nitrous oxide by nitrification and denitrification at constant temperature and moisture

 Soils are a major source of atmospheric NO and N₂O. Since the soil properties that regulate the production and consumption of NO and N₂O are still largely unknown, we studied N trace gas turnover by nitrification and denitrification in 20 soils as a function of various soil variables. Since fertilizer treatment, temperature and moisture are already known to affect N trace gas turnover, we avoided the masking effect of these soil variables by conducting the experiments in non-fertilized soils at constant temperature and moisture. In all soils nitrification was the dominant process of NO production, and in 50% of the soils nitrification was also the dominant process of N₂O production. Factor analysis extracted three factors which together explained 71% of the variance and identified three different soil groups. Group I contained acidic soils, which showed only low rates of microbial respiration and low contents of total and inorganic nitrogen. Group II mainly contained acidic forest soils, which showed relatively high respiration rates and high contents of total N and NH₄ ⁺. Group III mainly contained neutral agricultural soils with high potential rates of nitrification. The soils of group I produced the lowest amounts of NO and N₂O. The results of linear multiple regression conducted separately for each soil group explained between 44–100% of the variance. The soil variables that regulated consumption of NO, total production of NO and N₂O, and production of NO and N₂O by either nitrification or denitrification differed among the different soil groups. The soil pH, the contents of NH₄ ⁺, NO₂ ^– and NO₃ ^–, the texture, and the rates of microbial respiration and nitrification were among the important variables. Received: 28 October 1999     

Nitrous oxide emissions and methane oxidation by soil following cultivation of two different leguminous pastures

 Nitrous oxide (N₂O) emissions and methane (CH₄) consumption were quantified following cultivation of two contrasting 4-year-old pastures. A clover sward was ploughed (to 150–200 mm depth) while a mixed herb ley sward was either ploughed (to 150–200 mm depth) or rotovated (to 50 mm depth). Cumulative N₂O emissions were significantly greater following ploughing of the clover sward, with 4.01 kg N₂O-N ha^–1 being emitted in a 48-day period. Emissions following ploughing and rotovating of the ley sward were much less and were not statistically different from each other, with 0.26 and 0.17 kg N₂O-N ha^–1 being measured, respectively, over a 55-day period. The large difference in cumulative N₂O between the clover and ley sites is presumably due to the initially higher soil NO₃ ^– content, greater water filled pore space and lower soil pH at the clover site. Results from a denitrification enzyme assay conducted on soils from both sites showed a strong negative relationship (r=–0.82) between soil pH and the N₂O:(N₂O+N₂) ratio. It is suggested that further research is required to determine if control of soil pH may provide a relatively cheap mitigation option for N₂O emissions from these soils. There were no significant differences in CH₄ oxidation rates due to sward type or form of cultivation. Received: 1 November 1998     

Factors influencing nitrous oxide and methane emissions from minerotrophic fens in northeast Germany

 At two field sites representing northeastern German minerotrophic fens (Rhin-Havelluch, a shallow peat site; Gumnitz, a partially drained peat site) the influence of different factors (N fertilization, groundwater table, temperature) on N₂O and CH₄ emissions was investigated. The degraded fens were sources or sinks of the radiatively active trace gases investigated. The gas fluxes measured were much higher than those found in other terrestrical ecosystems such as forests. Lowering the groundwater table increased the release of N₂O and the oxidation of CH₄. High CH₄ emission rates occurred when the groundwater tables and soil temperatures were high (>12  °C). N fertilization stimulated the release of N₂O only when application rates were very high (480 kg N ha^–1). A moderate N supply (60 or 120 kg N ha^–1) hardly increased the release of N₂O in spite of high soluble soil NO₃ ^– contents. Received: 31 October 1997     

Mineralization and denitrification in upland, nearly saturated and flooded subtropical soil II. Effect of organic manures varying in N content and C:N ratio

 Nitrogen and carbon mineralization of cattle manure (N=6 g kg^–1; C:N=35), pressmud (N=17.4 g kg^–1; C:N=22), green manure (N=26.8 g kg^–1; C:N=14) and poultry manure (N=19.5 g kg^–1; C:N=12) and their influence on gaseous N losses via denitrification (using the acetylene inhibition technique) in a semiarid subtropical soil (Typic Ustochrepts) were investigated in a growth chamber simulating upland, nearly saturated, and flooded conditions. Mineralization of N started quickly in all manures, except pressmud where immobilization of soil mineral N was observed for an initial 4 days. Accumulation of mineral N in upland soil plus denitrified N revealed that mineralization of cattle manure-, pressmud-, poultry manure- and green manure-N over 16 days was 12, 20, 29 and 44%, respectively, and was inversely related to C:N ratio (R ²=0.703, P=0.05) and directly to N content of organic manure (R ²=0.964, P=0.01). Manure-C mineralized over 16 days ranged from 6% to 50% in different manures added to soil under different moisture regimes and was, in general, inversely related to initial C:N ratio of manure (R ²=0.690, P=0.05). Cumulative denitrification losses over 16 days in control soils (without manure) under upland, nearly saturated, and flooded conditions were 5, 23, and 24 mg N kg^–1, respectively. Incorporation of manures enhanced denitrification losses by 60-82% in upland, 52–163% in nearly saturated, and 26–107% in flooded soil conditions over a 16-day period, demonstrating that mineralized N and C from added manures could result in 2- to 3-fold higher rate of denitrification. Cumulative denitrification losses were maximal with green manure, followed by poultry manure, pressmud and cattle manure showing an increase in denitrification with increasing N content and decreasing C:N ratio of manure. Manure-amended nearly saturated soils supported 14–35% greater denitrification than flooded soils due to greater mineralization and supply of C.     

Effect of three contrasting onion (Allium cepa L.) production systems on nitrous oxide emissions from soil

 N₂O emissions were measured from three contrasting onion (Allium cepa L.) production systems over an 8.5-month period. One system was established on soil where a clover sward had 3 months earlier been ploughed in (ploughed clover site). This production system followed conventional production management practices. The other two systems were established on soil where a mixed herb ley had 3 months earlier been either ploughed or rotovated. These last two production systems followed the guidelines of the International Federation of Organic Agriculture Movements (IFOAM). Cumulative N₂O emissions were significantly greater from the ploughed clover site compared to the ploughed ley site (3.8 and 1.6 kg N₂O-N ha^–1, respectively), while cumulative N₂O emissions from the ploughed ley and rotovated ley sites were not significantly different from each other. Emissions from all sites were dominated by episodes of high N₂O flux activity following seedbed preparation and drilling, when soil water suction (SWS) was shown to be the rate-controlling variable. The decline in the N₂O fluxes after these peak emissions followed clear exponential relationships of the form F=Ae^{– kt} (r≥0.91), where F is the daily flux and A is the y-intercept. First-order decay constants (k) during these periods of declining N₂O fluxes (corresponding to half-lives of 2.6–3.0 days) were not significantly different in magnitude from the first-order rate constants that characterised the increasing SWS. Gross differences in cumulative emissions between the clover and ley sites were attributed to the influence of differing soil pHs at the two sites on the N₂O:(N₂O+N₂) ratio in the denitrification products. It also appeared that fertiliser applications to the clover site had both direct and indirect effects on N₂O emissions by: (1) enhancing N₂O emissions via potential nitrification, (2) increasing the NO₃ ^– supply for enhanced N₂O emissions via denitrification, and (3) influencing the N₂O:(N₂O+N₂) ratio by lowering soil pH and increasing NO₃ ^– concentrations. Onion crop yields were greater at the clover site, mainly due to the higher density of planting made possible under a conventional production philosophy. Expressing the yield on the basis of net N₂O emissions, 23 t onions kg^–1 N₂O-N was obtained from the ploughed clover, which was double that obtained for the two systems based on the ley site. However, when the N₂O emissions from the cultivation of the soils prior to the sowing of the onions was included, all three systems produced a similar yield per kilogram of N₂O-N emitted, averaging 10 t kg^–1. Received: 6 January 1999     

Perchlorate Depositional History as Recorded in North American Ice Cores from the Eclipse Icefield, Canada, and the Upper Fremont Glacier, USA

Temporal depositional rates are important in order to understand the production and occurrence of perchlorate (ClO₄⁻) as limited information exists regarding the impact of anthropogenic production or atmospheric pollution on ClO₄⁻ deposition. Perchlorate concentrations in discrete ice core samples from the Eclipse Icefield (Yukon Territory, Canada) and Upper Fremont Glacier (Wyoming, USA) were analyzed using ion chromatography tandem mass spectrometry to evaluate temporal changes in the deposition of ClO₄ ⁻ in North America. The ice core samples cover a time period from 1726 to 1993 and 1970 to 2002 for the Upper Fremont Glacier (UFG) and Eclipse ice cores, respectively. The average ClO₄ ⁻ concentration in the Eclipse ice core for the time period from 1970 to 1973 was 0.6 ± 0.3 ng L⁻¹, with higher values of 2.3 ± 1.7 and 2.2 ± 2.0 ng L⁻¹ for the periods 1982–1986 and 1999–2002, respectively. All pre-1980 ice core samples from the UFG had ClO₄ ⁻ concentrations <0.2 ng L⁻¹, and the post-1980 samples ranged from <0.2 ng L⁻¹ to a maximum of 2.6 ng L⁻¹ for the year 1992. A significant positive correlation (R = 0.75, N = 15, p < 0.001) of ClO₄⁻ with SO₄²⁻ was found for the annual UFG ice core layers and of ClO₄ ⁻ with SO₄²⁻ and NO₃⁻ in sub-annual Eclipse ice samples (R > 0.3, N = 121, p < 0.002). The estimated yearly ClO₄⁻ depositional flux for the Eclipse ice core ranged from 0.6 (1970) to 4.7 μg m⁻² year⁻¹ (1982) and the UFG from <0.1 (pre-1980) to 1.4 μg m⁻² year⁻¹ (1992). There was no consistent seasonal variation in the ClO₄⁻ depositional flux for the Eclipse ice core, in contrast to a previous study on the Arctic region. The presence of ClO₄⁻ in these ice cores might correspond to an intermittent source such as volcanic eruptions and/or any anthropogenic forcing that may directly or indirectly aid in atmospheric ClO₄⁻ formation.